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Hypocomplementemic Urticarial Vasculitis Syndrome with Membranous Nephropathy: Case Report
Su Woong Jung1, Yun Young Choi2, In Seung Choi2
1Department of Medicine, Graduate School, Kyung Hee University, Seoul, Korea.
Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare condition. This case study details a teenage boy with HUVS following influenza A, who later developed myositis and kidney complications.
Area of Science:
- Rheumatology
- Immunology
- Dermatology
Background:
- Urticarial vasculitis is a rare inflammatory disorder characterized by recurrent urticarial lesions, potentially involving systemic organs.
- Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a subtype often associated with low complement levels.
- Systemic involvement can manifest at disease onset or develop over time, impacting joints, kidneys, lungs, and eyes.
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